CN107431001A - Semiconductor element and its manufacture method - Google Patents
Semiconductor element and its manufacture method Download PDFInfo
- Publication number
- CN107431001A CN107431001A CN201680019663.5A CN201680019663A CN107431001A CN 107431001 A CN107431001 A CN 107431001A CN 201680019663 A CN201680019663 A CN 201680019663A CN 107431001 A CN107431001 A CN 107431001A
- Authority
- CN
- China
- Prior art keywords
- lateral electrode
- back side
- semiconductor element
- electrode
- phosphorus
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 239000004065 semiconductor Substances 0.000 title claims abstract description 100
- 238000000034 method Methods 0.000 title claims description 75
- 238000004519 manufacturing process Methods 0.000 title claims description 20
- 239000011248 coating agent Substances 0.000 claims abstract description 65
- 238000000576 coating method Methods 0.000 claims abstract description 65
- OFNHPGDEEMZPFG-UHFFFAOYSA-N phosphanylidynenickel Chemical compound [P].[Ni] OFNHPGDEEMZPFG-UHFFFAOYSA-N 0.000 claims abstract description 61
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims abstract description 44
- 229910052737 gold Inorganic materials 0.000 claims abstract description 43
- 239000010931 gold Substances 0.000 claims abstract description 43
- 239000000758 substrate Substances 0.000 claims abstract description 43
- 238000007772 electroless plating Methods 0.000 claims abstract description 39
- 229910000838 Al alloy Inorganic materials 0.000 claims abstract description 27
- 239000004411 aluminium Substances 0.000 claims abstract description 25
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 25
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 25
- 238000007747 plating Methods 0.000 claims description 47
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 39
- 229910052698 phosphorus Inorganic materials 0.000 claims description 39
- 239000011574 phosphorus Substances 0.000 claims description 39
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 claims description 22
- 239000000463 material Substances 0.000 claims description 18
- 229910000679 solder Inorganic materials 0.000 abstract description 20
- 238000005476 soldering Methods 0.000 abstract description 12
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 28
- 230000008569 process Effects 0.000 description 26
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 16
- 229910052725 zinc Inorganic materials 0.000 description 16
- 239000011701 zinc Substances 0.000 description 16
- 229910052759 nickel Inorganic materials 0.000 description 14
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 10
- 239000002253 acid Substances 0.000 description 9
- 238000010276 construction Methods 0.000 description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
- 230000015572 biosynthetic process Effects 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 230000008859 change Effects 0.000 description 7
- 238000005238 degreasing Methods 0.000 description 7
- 239000012530 fluid Substances 0.000 description 6
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 6
- 229910052763 palladium Inorganic materials 0.000 description 5
- 238000005554 pickling Methods 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 238000005219 brazing Methods 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 239000003638 chemical reducing agent Substances 0.000 description 3
- 229910017052 cobalt Inorganic materials 0.000 description 3
- 239000010941 cobalt Substances 0.000 description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 3
- 238000009792 diffusion process Methods 0.000 description 3
- 238000005530 etching Methods 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229910052697 platinum Inorganic materials 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- 239000010703 silicon Substances 0.000 description 3
- 229910052709 silver Inorganic materials 0.000 description 3
- 239000004332 silver Substances 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000006555 catalytic reaction Methods 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- 238000009713 electroplating Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000011133 lead Substances 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229910017604 nitric acid Inorganic materials 0.000 description 2
- 239000005416 organic matter Substances 0.000 description 2
- 230000033116 oxidation-reduction process Effects 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 229910052718 tin Inorganic materials 0.000 description 2
- 239000011135 tin Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910000967 As alloy Inorganic materials 0.000 description 1
- 229910001218 Gallium arsenide Inorganic materials 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000008139 complexing agent Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000013527 degreasing agent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- BBKFSSMUWOMYPI-UHFFFAOYSA-N gold palladium Chemical compound [Pd].[Au] BBKFSSMUWOMYPI-UHFFFAOYSA-N 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L24/00—Arrangements for connecting or disconnecting semiconductor or solid-state bodies; Methods or apparatus related thereto
- H01L24/01—Means for bonding being attached to, or being formed on, the surface to be connected, e.g. chip-to-package, die-attach, "first-level" interconnects; Manufacturing methods related thereto
- H01L24/02—Bonding areas ; Manufacturing methods related thereto
- H01L24/04—Structure, shape, material or disposition of the bonding areas prior to the connecting process
- H01L24/05—Structure, shape, material or disposition of the bonding areas prior to the connecting process of an individual bonding area
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/16—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
- C23C18/1601—Process or apparatus
- C23C18/1633—Process of electroless plating
- C23C18/1635—Composition of the substrate
- C23C18/1637—Composition of the substrate metallic substrate
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/16—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
- C23C18/1601—Process or apparatus
- C23C18/1633—Process of electroless plating
- C23C18/1646—Characteristics of the product obtained
- C23C18/165—Multilayered product
- C23C18/1651—Two or more layers only obtained by electroless plating
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- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/16—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
- C23C18/18—Pretreatment of the material to be coated
- C23C18/1803—Pretreatment of the material to be coated of metallic material surfaces or of a non-specific material surfaces
- C23C18/1824—Pretreatment of the material to be coated of metallic material surfaces or of a non-specific material surfaces by chemical pretreatment
- C23C18/1837—Multistep pretreatment
- C23C18/1844—Multistep pretreatment with use of organic or inorganic compounds other than metals, first
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- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/16—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
- C23C18/31—Coating with metals
- C23C18/32—Coating with nickel, cobalt or mixtures thereof with phosphorus or boron
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- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
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- C23C18/31—Coating with metals
- C23C18/32—Coating with nickel, cobalt or mixtures thereof with phosphorus or boron
- C23C18/34—Coating with nickel, cobalt or mixtures thereof with phosphorus or boron using reducing agents
- C23C18/36—Coating with nickel, cobalt or mixtures thereof with phosphorus or boron using reducing agents using hypophosphites
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- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/16—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
- C23C18/31—Coating with metals
- C23C18/42—Coating with noble metals
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- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/28—Manufacture of electrodes on semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/268
- H01L21/283—Deposition of conductive or insulating materials for electrodes conducting electric current
- H01L21/288—Deposition of conductive or insulating materials for electrodes conducting electric current from a liquid, e.g. electrolytic deposition
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- H01L24/03—Manufacturing methods
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- C—CHEMISTRY; METALLURGY
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- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/54—Contact plating, i.e. electroless electrochemical plating
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- H01L2224/04026—Bonding areas specifically adapted for layer connectors
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- H01L2224/05099—Material
- H01L2224/051—Material with a principal constituent of the material being a metal or a metalloid, e.g. boron [B], silicon [Si], germanium [Ge], arsenic [As], antimony [Sb], tellurium [Te] and polonium [Po], and alloys thereof
- H01L2224/05117—Material with a principal constituent of the material being a metal or a metalloid, e.g. boron [B], silicon [Si], germanium [Ge], arsenic [As], antimony [Sb], tellurium [Te] and polonium [Po], and alloys thereof the principal constituent melting at a temperature of greater than or equal to 400°C and less than 950°C
- H01L2224/05124—Aluminium [Al] as principal constituent
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Abstract
The semiconductor element (1) of the present invention is in the surface lateral electrode (3a) and back side lateral electrode (3b) of surface back side conducting type substrate (2) formed with non-electrolytic nickel-phosphorus coating (4) and electroless plating layer gold (5).Surface lateral electrode (3a) and back side lateral electrode (3b) include aluminium or aluminium alloy.In addition, the thickness for the non-electrolytic nickel-phosphorus coating (4) being formed in surface lateral electrode (3a) is more than 1.0 and less than 3.5 relative to the ratio of the thickness for the non-electrolytic nickel-phosphorus coating (4) being formed in back side lateral electrode (3b).The semiconductor element (1) of the present invention can prevent from producing emptying aperture inside solder when installing by soldering.
Description
Technical field
The present invention relates to semiconductor element and its manufacture method.Specifically, the present invention relates to surface back side conducting type
Semiconductor element, the power converter more particularly to IGBT (insulated gate bipolar transistor), diode etc. for representative
Power semiconductor and its manufacture method.
Background technology
In the past, in the case of by the semiconductor element mounting of surface back side conducting type to module, the back of the body of semiconductor element
Surface side electrode is soldered to substrate etc., and the surface lateral electrode of semiconductor element is by wire bonding.However, in recent years, according to shortening
Manufacturing time and the viewpoint for cutting down fee of material, use the peace of the direct brazing metal electrode of surface lateral electrode to semiconductor element
The situation of dress method becomes more.The surface lateral electrode of semiconductor element generally comprises aluminium or aluminium alloy, so in order to carry out soldering,
Need to form nickel film, golden film etc. in the surface lateral electrode of semiconductor element.
Nickel film reacts in soldering and reduced with the solder of tin system, so needing to make nickel film by several μm of horizontal thick film
Change.However, in the case where using the vacuum film formation mode such as evaporation or sputtering, generally, maximum can only obtain 1.0 μm or so
Thickness.In addition, if wanting forcibly to make nickel thickness membranization, then manufacturing cost rises.Therefore, as can realize it is low into
Originally, the film build method of high speed and thick-film, plating technique are attracted attention.
As plating technique, existing can be only in electrode (hereinafter referred to as " Al electrodes ") table including aluminium or aluminium alloy
The non-electrolytic plating of plating layer is formed selectively on face.As non-electrolytic plating, typically palladium chtalyst method and zinc are utilized
Hydrochlorate method.
In palladium chtalyst method, palladium is separated out on the surface of Al electrodes as catalyst core, form electroless plating coating.
In palladium method, the etch quantity of Al electrodes is few, and the flatness on the surface of electroless plating coating is good, on the other hand, because your gold palladium is
Category, so manufacturing cost rises.
In addition, in zincate method, by making zinc be replaced with Al to be separated out as catalyst core on the surface of Al electrodes, shape
Into electroless plating coating.The zincic acid saline solution used in the method is cheap, so being widely adopted.
In fact, in patent document 1, it is proposed that selected on the surface of the Al electrodes of semiconductor element by zincate method
Form nickel coating and Gold plated Layer to property.
Prior art literature
Patent document 1:Japanese Unexamined Patent Publication 2005-51084 publications
The content of the invention
In the case of by the semiconductor element mounting of surface back side conducting type to module, place weld in substrate at normal temperatures
Material, and after also semiconductor element is placed thereon, heated with reflow ovens, so as to by the back side lateral electrode of semiconductor element
It is soldered to substrate.Now, the scaling powder in solder, be formed at the hydrogen included in the electroplated film of electrode or moisture etc. and be used as gas
Produce.If these gases keep remaining in inside solder, as emptying aperture (hole).Emptying aperture inside solder hinders electrical conduction
Or heat transfer, so the reason for action as generation semiconductor element is bad.In order to remove emptying aperture inside solder, it is necessary to
Micro-vibration etc. is applied to semiconductor element in soldering, but in the case of by multiple semiconductor element mountings to substrate, needed
Complicated device is wanted, and productivity ratio also reduces.
The present invention completes to solve the problems, such as above-mentioned, and its object is to provide one kind to install by soldering
When, can prevent inside solder produce emptying aperture semiconductor element and its manufacture method.
Present inventor carries out wholwe-hearted research discovery afterwards to solve the above problems, and electrode and plating are used by selection
The material of layer, and the thickness of plating layer is controlled, have before the brazing in a manner of the surface for making semiconductor element is in inner side
Meaning ground makes semiconductor element warpage, thereby, it is possible to easily be discharged to the outside the emptying aperture inside solder, and completes the present invention.
That is, the present invention provides a kind of semiconductor element, surface lateral electrode and the back side in surface back side conducting type substrate
It is characterised by lateral electrode formed with non-electrolytic nickel-phosphorus coating and electroless plating layer gold, the semiconductor element, the table
Surface side electrode and the back side lateral electrode include aluminium or aluminium alloy, also, are formed at described in the surface lateral electrode
The ratio of the thickness of the relative non-electrolytic nickel-phosphorus coating being formed in the back side lateral electrode of the thickness of non-electrolytic nickel-phosphorus coating
Example is more than 1.0 and less than 3.5.
In addition, the present invention provides a kind of manufacture method of semiconductor element, by surface lateral electrode and back side lateral electrode
It is formed at after surface back side conducting type substrate, using zincate method, to the surface lateral electrode and the back side lateral electrode
This two side carries out electroless phosphorus plating and electroless plating gold simultaneously, and the feature of the manufacture method of the semiconductor element exists
Include aluminium or aluminium alloy in, the surface lateral electrode and the back side lateral electrode, also, by the table of the surface lateral electrode
Area is set to more than 0.3 and less than 0.85 relative to the ratio of the surface area of the back side lateral electrode.
In accordance with the invention it is possible to provide the semiconductor that can prevent that emptying aperture is produced inside solder when being installed by soldering
Element and its manufacture method.
Brief description of the drawings
Fig. 1 is the profile of the semiconductor element of embodiment 1.
Fig. 2 is the figure for illustrating the method for a non-electrolytic nickel phosphor plating.
Fig. 3 is the figure for illustrating the method for another non-electrolytic nickel phosphor plating.
Fig. 4 is the figure for illustrating the method for another non-electrolytic nickel phosphor plating.
(symbol description)
1:Semiconductor element;2:Surface back side conducting type substrate;3a:Surface lateral electrode;3b:Back side lateral electrode;4:Non-electrical
Solve nickel-phosphorus coating;5:Electroless plating layer gold;6:Diaphragm;10:Electroless phosphorus plating solution;11:Dummy material.
Embodiment
Hereinafter, using accompanying drawing, the semiconductor element of the present invention and its preferred embodiment of manufacture method are illustrated.
Embodiment 1.
Fig. 1 is the profile of the semiconductor element of present embodiment.
In Fig. 1, the semiconductor element 1 of present embodiment includes surface back side conducting type substrate 2, is formed at surface back side
The surface lateral electrode 3a of one interarea (surface) of conducting type substrate 2, another master for being formed at surface back side conducting type substrate 2
The back side lateral electrode 3b in face (back side), the non-electrolytic nickel-phosphorus coating 4 formed on surface lateral electrode 3a and back side lateral electrode 3b
And it is formed at the electroless plating layer gold 5 on non-electrolytic nickel-phosphorus coating 4.In addition, it is provided with diaphragm on the lateral electrode 3a of surface
6。
The semiconductor element 1 of present embodiment is characterised by, in order to be prevented when being installed by soldering inside solder
Emptying aperture is produced, intentionally sticks up semiconductor element 1 in a manner of the surface for making semiconductor element 1 is in inner side before the brazing
It is bent.In addition, in Fig. 1, the warpage of semiconductor element 1 is not shown.
In order to apply warpage to semiconductor element 1, it is necessary to system will be expanded with the line bigger than surface back side conducting type substrate 2
Several electrodes and plating layer, which are set, arrives surface back side conducting type substrate 2.Therefore, in the semiconductor element 1 of present embodiment,
As electrode, selection includes the surface lateral electrode 3a and back side lateral electrode 3b of aluminium or aluminium alloy, as plating layer, selects non-
It is electrolysed nickel-phosphorus coating 4 and electroless plating layer gold 5.In addition, it is generally used for the line expansion system of the silicon of surface back side conducting type substrate 2
Number is about 2.3ppm/ DEG C, in contrast, the linear expansion coefficient of aluminium is about 23ppm/ DEG C, the linear expansion coefficient of nickel phosphorus is about 12~
13ppm/ DEG C, golden linear expansion coefficient is about 14.2ppm/ DEG C.
Next, the surface of semiconductor element 1 is set to be in the warpage of inner side, it is necessary to make in order to apply to semiconductor element 1
The electrode on the surface of semiconductor element 1 and the thickness of plating layer are more than the electrode and plating layer at the back side of semiconductor element 1
Thickness.Wherein, according to the viewpoint of the productivity ratio of semiconductor element 1, be preferably controlled in electrode and plating layer it is most thick simultaneously
And it is easily controlled the thickness of the non-electrolytic nickel-phosphorus coating 4 of thickness.Therefore, the non-electrolytic nickel phosphor plating for being formed at surface lateral electrode 3a is made
The thickness of layer 4 is more than the thickness for the non-electrolytic nickel-phosphorus coating 4 being formed on the lateral electrode 3b of the back side.
In particular, it is desirable to the thickness for the non-electrolytic nickel-phosphorus coating 4 for making to be formed on the lateral electrode 3a of surface is relative to formation
In the non-electrolytic nickel-phosphorus coating 4 on the lateral electrode 3b of the back side thickness ratio for more than 1.0 and less than 3.5, preferably 1.05 with
It is upper and less than 3.5, more preferably more than 1.2 and less than 3.4.When the ratio is less than 1.0, the warpage of semiconductor element 1 is not filled
Point, emptying aperture is produced inside solder in soldering.On the other hand, when the ratio is more than 3.5, the warpage of semiconductor element 1 becomes
Too much, warpage residues in semiconductor element 1 after the brazing.
As surface back side conducting type substrate 2, it is not particularly limited, Si substrates, SiC substrate, GaAs chemical combination can be used
The known semiconductor substrate in the technical field such as thing system substrate.There is surface back side conducting type substrate 2 diffusion layer (not scheme
Show), possess the function of controlling the actions of semiconductor element 1 such as PN junction, gate electrode.
As described above, surface lateral electrode 3a and back side lateral electrode 3b includes aluminium or aluminium alloy.
As aluminium alloy, it is not particularly limited, the known material in the technical field can be used.Aluminium alloy preferably contains
There is the element of (noble) more expensive than aluminium.By the way that containing the element more expensive than aluminium, electroless phosphorus plating is being carried out using zincate method
When, electronics is easily from the existing aluminium outflow around the element, so promoting the dissolving of aluminium.In addition, aluminium dissolving part,
Zinc intensively separates out, and the precipitation quantitative change as the zinc for the starting point for forming non-electrolytic nickel-phosphorus coating 4 is more, so easily forming non-electrolytic
Nickel-phosphorus coating 4.
As the element more expensive than aluminium, be not particularly limited, for example, can enumerate iron, nickel, tin, lead, silicon, copper, silver, gold,
Tungsten, cobalt, platinum, palladium, iridium, rhodium etc..In these elements, preferably copper, silicon, iron, nickel, silver, gold.In addition, these elements can be single
Solely use or combine two or more use.
The content of the expensive element of ratio aluminium in aluminium alloy is not particularly limited, preferably below 5 mass %, more preferably
More than 0.05 mass % and below 3 mass %, more preferably more than 0.1 mass % and below 2 mass %.
The element expensive for the ratio aluminium contained in surface lateral electrode 3a and the back side lateral electrode 3b aluminium alloy both can phase
Together can also be different.However, rear side is being formed by the element ratio for making to contain in the aluminium alloy for forming surface lateral electrode 3a
The element contained in electrode 3b aluminium alloy is expensive, easily makes the thickness for being formed at surface lateral electrode 3a non-electrolytic nickel-phosphorus coating 4
More than the thickness for the non-electrolytic nickel-phosphorus coating 4 being formed on the lateral electrode 3b of the back side.
Surface lateral electrode 3a and the back side lateral electrode 3b thickness are not particularly limited, and apply according to semiconductor element 1
Make semiconductor element 1 surface be in inner side warpage viewpoint, preferably surface lateral electrode 3a thickness is more than back side lateral electrode
3b thickness.
Surface lateral electrode 3a thickness is in general 1 μm~8 μm, preferably 2 μm~7 μm, more preferably 3 μm~6 μm.
Back side lateral electrode 3b thickness is in general 0.1 μm~4 μm, preferably 0.5 μm~3 μm, more preferably 0.8 μm
~2 μm.
The non-electrolytic nickel-phosphorus coating 4 formed on surface lateral electrode 3a and back side lateral electrode 3b is not particularly limited, energy
Enough use the material of various compositions.
Phosphorus concentration in non-electrolytic nickel-phosphorus coating 4 is in general below 15 mass %, the matter of preferably 1 mass %~12
Measure %, the mass % of more preferably 3 mass %~10.Phosphorus concentration in the non-electrolytic nickel-phosphorus coating 4 is in non-electrolytic nickel-phosphorus coating 4
Thickness it is more thick, become lower tendency.
The thickness of the non-electrolytic nickel-phosphorus coating 4 formed on surface lateral electrode 3a and back side lateral electrode 3b is as long as there is upper
The ratio of bright thickness is stated, is not particularly limited.
The thickness for the non-electrolytic nickel-phosphorus coating 4 being formed on the lateral electrode 3a of surface is in general 3 μm~10 μm, is preferably
4 μm~9 μm, more preferably 3 μm~8 μm.
The thickness for the non-electrolytic nickel-phosphorus coating 4 being formed on the lateral electrode 3b of the back side is in general 1 μm~7 μm, is preferably
1.5 μm~6 μm, more preferably 2 μm~5 μm.
The thickness for the electroless plating layer gold 5 being formed on non-electrolytic nickel-phosphorus coating 4 is not particularly limited, it is however generally that is
Less than 0.1 μm, preferably 0.01 μm~0.08 μm, more preferably 0.02 μm~0.05 μm.
In addition, the surface for making semiconductor element 1 according to applying to semiconductor element 1 is in the viewpoint of the warpage of inner side, table
The thickness of the electroless plating layer gold 5 in face is preferably greater than the thickness of the electroless plating layer gold 5 at the back side.
As diaphragm 6, it is not particularly limited, the known example in the technical field can be used.
Semiconductor element 1 with above-mentioned construction is in the warpage of inner side with making the surface of semiconductor element 1.
Specifically, the amount of warpage of semiconductor element 1 is preferably 0.2mm~2mm, more preferably 0.3mm~1.8mm, is entered
One step is preferably 0.4mm~1.6mm.If the amount of warpage of such scope, then semiconductor device 1 is being installed by soldering
When, it can prevent from producing emptying aperture inside solder.
Here, the amount of warpage of semiconductor element 1 means make the backside down of semiconductor element 1 be configured on platform
When the distance away from platform surface of the end of semiconductor element 1 that tilts.
After surface lateral electrode 3a and back side lateral electrode 3b are formed at into surface back side conducting type substrate 2, zinc is used
Hydrochlorate method, electroless phosphorus plating and electroless plating are carried out simultaneously to surface lateral electrode 3a and this two side of back side lateral electrode 3b
Gold, so as to manufacture the semiconductor element 1 with above-mentioned construction.
In order to carry out electroless phosphorus plating simultaneously to surface lateral electrode 3a and this two side of back side lateral electrode 3b and half-and-half
Conductor element 1, which applies, makes the surface of semiconductor element 1 be in the warpage of inner side, it is necessary to make surface lateral electrode 3a surface area relative
In back side lateral electrode 3b surface area ratio be more than 0.3 and less than 0.85, preferably more than 0.5 and less than 0.85, it is more excellent
Elect more than 0.6 and less than 0.8 as.
Specifically, as shown in Fig. 2 by formed with surface area different surface lateral electrode 3a's and back side lateral electrode 3b
Surface back side conducting type substrate 2 is impregnated into electroless phosphorus plating solution 10.In addition, in fig. 2, omit diaphragm 6.Pass through
Above-mentioned difference is set to surface lateral electrode 3a and the back side lateral electrode 3b surface area, surface lateral electrode 3a and rear side can be made
The formation velocity variations of non-electrolytic nickel-phosphorus coating 4 at electrode 3b, so can be in surface lateral electrode 3a and back side lateral electrode
The different non-electrolytic nickel-phosphorus coating 4 of thickness is formed at 3b.
In addition, the in order that formation speed of the non-electrolytic nickel-phosphorus coating 4 at surface lateral electrode 3a and back side lateral electrode 3b
Change, can also make bath (bath) load variations.Here, bath load means that the electrode of electroless phosphorus plating will be carried out
Surface area (dm2) divided by the capacity (L) of plating solution obtained from value.Surface lateral electrode 3a bath load is preferably 0.2dm2/
L~2dm2/ L, more preferably 0.3dm2/ L~1.5dm2/L.Back side lateral electrode 3b bath load is preferably 1.0dm2/ L~
10dm2/ L, more preferably 2.0dm2/ L~9.0dm2/L。
In addition, the in order that formation speed of the non-electrolytic nickel-phosphorus coating 4 at surface lateral electrode 3a and back side lateral electrode 3b
Change, can also be as shown in figure 3, carry out electroless phosphorus in the position configuration dummy material 11 opposed with back side lateral electrode 3b
Plating.In addition, in figure 3, omit diaphragm 6.Electroless phosphorus plating is carried out by using such method, surface can be increased
The difference of the formation speed of non-electrolytic nickel-phosphorus coating 4 between lateral electrode 3a and back side lateral electrode 3b.
As dummy material 11, as long as easily forming the material of non-electrolytic nickel-phosphorus coating 4, it is not particularly limited.Make
For the example of dummy material 11, iron, platinum, gold, nickel, cobalt, silver or their alloy etc. can be enumerated.In them, it is preferably
Iron, platinum, gold, nickel, cobalt.
Back side lateral electrode 3b and the distance of dummy material 11 are not particularly limited, preferably 2mm~20mm, more preferably
3mm~15mm, more preferably 4mm~12mm, most preferably 5mm~10mm.
In addition, the in order that formation speed of the non-electrolytic nickel-phosphorus coating 4 at surface lateral electrode 3a and back side lateral electrode 3b
Change, can also be as shown in figure 4, prepare to turn on formed with surface lateral electrode 3a and back side lateral electrode 3b multiple surface back sides
Type substrate 2, make the back side lateral electrode 3b of surface back side conducting type substrate 2 is opposite each other to carry out electroless phosphorus plating.In addition,
In Fig. 4, diaphragm 6 is omitted.By using such method carry out electroless phosphorus plating, can increase surface lateral electrode 3a with
The difference of the formation speed of non-electrolytic nickel-phosphorus coating 4 between the lateral electrode 3b of the back side, and can be to being turned in multiple surface back sides
The surface lateral electrode 3a and back side lateral electrode 3b that are formed on type substrate 2 while electroless phosphorus plating is carried out, so productivity ratio
Also improve.
The distance between back side lateral electrode 3b is not particularly limited, preferably 2mm~50mm, more preferably 3mm~40mm,
More preferably 4mm~35mm, most preferably 5mm~30mm.
As the method that surface lateral electrode 3a and back side lateral electrode 3b are formed at into surface back side conducting type substrate 2,
Known in the technical field, so the description thereof will be omitted, below explanation using zincate method electroless phosphorus plating and
Electroless plating gold.
When forming non-electrical on the surface lateral electrode 3a and back side lateral electrode 3b for being formed at surface back side conducting type substrate 2
In the case of solving nickel-phosphorus coating 4 and electroless plating layer gold 5, typically, carry out successively plasma clean process, degreasing process,
Pickling process, the first zincate treatment process, zincate stripping process, the second zincate treatment process, electroless phosphorus plating
Process, electroless plating gold process.Between each operation, should sufficiently it be washed, the treatment fluid or residue of process before preventing
It is brought into rear process.Hereinafter, the outline of each operation is illustrated.
In plasma clean process, surface lateral electrode 3a and the back of the body to being formed at surface back side conducting type substrate 2
Surface side electrode 3b carries out plasma clean.In order to carry out oxidation Decomposition etc. by using plasma, removal is firmly adhered to
Surface lateral electrode 3a and the back side lateral electrode 3b debris, nitride or oxide, and ensure surface lateral electrode
3a and back side lateral electrode 3b and the pretreatment liquid of plating or the reactivity of plating solution, carry out plasma clean.Plasma
Body cleaning is to surface lateral electrode 3a and back side lateral electrode 3b this two side progress, but preferably emphasis is carried out to surface lateral electrode 3a.
In addition, the order as plasma clean, is not particularly limited, plasma clean preferably is being carried out to back side lateral electrode 3b
Afterwards, plasma clean is carried out to surface lateral electrode 3a.The reason for this is that in the table side of semiconductor element 1, with face side electricity
The diaphragm 6 that is made up of organic matter together be present in pole 3a, the residue of the diaphragm 6 be attached to surface lateral electrode 3a situation compared with
It is more.
In degreasing process, surface lateral electrode 3a and back side lateral electrode 3b degreasing is carried out.Table is attached in order to remove
Slight organic matter, lubricant component, the oxide-film on surface side electrode 3a and the back side lateral electrode 3b surface, carry out degreasing.Typically
For, to surface lateral electrode 3a and back side lateral electrode 3b using the strong alkaline decoction of etching power, carry out degreasing.Pass through degreasing
Process, lubricant component are saponified.In addition, on the material not being saponified, the solvable material of alkali is dissolved into the decoction, and alkali is not
Solvable material is pulled away by surface lateral electrode 3a and the back side lateral electrode 3b etching.
In pickling process, pickling is carried out to surface lateral electrode 3a and back side lateral electrode 3b.In order to surface lateral electrode
3a and the back side lateral electrode 3b surface are neutralized and are roughened by etching, the treatment fluid after raising in process
Reactivity, the adhesive force of plating is improved, so as to carry out pickling.
In the first zincate treatment process, zincic acid salt treatment is carried out to surface lateral electrode 3a and back side lateral electrode 3b.
Here, zincic acid salt treatment refers to be etched oxide film dissolving of making a return journey on the surface to surface lateral electrode 3a and back side lateral electrode 3b
While formed zinc overlay film processing.In general, surface lateral electrode 3a and back side lateral electrode 3b are being impregnated into dissolving
When having the aqueous solution (the zincate treatment fluid) of zinc, due to compared to form surface lateral electrode 3a and back side lateral electrode 3b aluminium or
Person's aluminium alloy, the standard oxidationreduction potential of zinc is more expensive, so aluminium is as ion-solubility.By this caused electronics, zinc from
Son receives electronics at surface lateral electrode 3a and the back side lateral electrode 3b surface, lateral electrode 3a and back side lateral electrode on surface
3b surface forms the overlay film of zinc.
In zincate stripping process, by the surface lateral electrode 3a and back side lateral electrode of overlay film of the surface formed with zinc
3b is impregnated into nitric acid, dissolves zinc.
In the second zincate treatment process, by the surface lateral electrode 3a obtained by zincate stripping process and the back side
Lateral electrode 3b is impregnated into zincate treatment fluid again.Thus, removing aluminium and its while oxide-film, on surface lateral electrode 3a with
And back side lateral electrode 3b surface forms the overlay film of zinc.
The reasons why carrying out above-mentioned zincate stripping process and the second zincate treatment process is, makes surface lateral electrode 3a
And back side lateral electrode 3b surface is smoothened.In addition, the repetition time of zincate treatment process and zincate stripping process
Number is more, then surface lateral electrode 3a and the back side lateral electrode 3b surface are more smooth, forms more uniform non-electrolytic nickel-phosphorus coating 4
And electroless plating layer gold 5.But when considering the balance of surface smoothness and productivity ratio, preferably zincic acid salt treatment is carried out
Twice, more preferably carry out three times.
In electroless phosphorus plating process, by the way that the surface lateral electrode 3a and rear side of the overlay film formed with zinc is electric
Pole 3b is impregnated into electroless phosphorus plating solution 10, forms non-electrolytic nickel-phosphorus coating 4.The face side of the overlay film formed with zinc is electric
When pole 3a and back side lateral electrode 3b are impregnated into electroless phosphorus plating solution 10, initially, zinc is compared to nickel, standard oxidation reduction electricity
Position is low-priceder, so nickel separates out on surface lateral electrode 3a and back side lateral electrode 3b.Next, when being covered on surface by nickel, lead to
The effect of the reducing agent included is crossed in electroless phosphorus plating solution 10, is separated out to nickel self-catalysis.In the precipitation of the self-catalysis,
The composition of reducing agent (hypophosphorous acid) is introduced in electroplated film, so forming the non-electrolytic nickel-phosphorus coating 4 as alloy.In addition,
When the concentration of reducing agent is high, non-electrolytic nickel-phosphorus coating 4 turns into noncrystal.In addition, persistently produced all the time in electroless phosphorus plating
Raw hydrogen, so the occlusion hydrogen in non-electrolytic nickel-phosphorus coating 4.
In electroless plating gold process, by the surface lateral electrode 3a formed with non-electrolytic nickel-phosphorus coating 4 and the back side
Lateral electrode 3b carries out electroless plating gold, forms electroless plating layer gold 5.In general, carried out by the method for being referred to as displaced type
Electroless plating gold.By using the effect of the complexing agent included in electroless plating gold liquid, nickel and the gold of non-electrolytic nickel-phosphorus coating 4
Enter line replacement, so as to carry out the electroless plating gold of displaced type.In addition, surface quilt of the electroless plating gold in non-electrolytic nickel-phosphorus coating 4
Reaction stops during gold covering, so being difficult to make electroless plating layer gold 5 thickening, its thickness maximum is 0.08 μ, is in general 0.08
μm or so.But as soldering purposes, come in the case of utilizing, the even above-mentioned value of thickness of electroless plating layer gold 5 is not yet
Can be too small.
Embodiment
Hereinafter, by embodiment, the present invention is described in detail, but the present invention is not limited to this.
(embodiment 1)
In embodiment 1, the semiconductor element 1 with the construction shown in Fig. 1 is made.
First, as surface back side conducting type substrate 2, the thickness for preparing diffusion layer be 70 μm Si substrates (14mm ×
14mm)。
Next, on the surface of Si substrates, the aluminium electrode (5 μm of thickness) and diaphragm as surface lateral electrode 3a are formed
6, at the back side of Si substrates, form the aluminium electrode (1 μm of thickness) as back side lateral electrode 3b.Here, by surface lateral electrode 3a's
Surface area is set to 0.60 relative to the ratio of back side lateral electrode 3b surface area.
Next, by carrying out each operation under conditions of shown in following tables 1, semiconductor element 1 is obtained.It is in addition, logical
The method shown in Fig. 2 is crossed, carries out electroless phosphorus plating.In addition, between each operation, the washing using pure water is carried out.
[table 1]
Process | Project | Condition etc. |
1 | Plasma clean | Ar (100cc/ minutes), 800W, 2 minutes, vacuum IOPa |
2 | Degreasing | Alkaline degreaser, pH9.5,70 DEG C, 3 minutes |
3 | Pickling | 10% sulfuric acid, 30 DEG C, 1 minute |
4 | First zincic acid salt treatment | Alkaline zincate treatment fluid, pH12,25 DEG C, 20 seconds |
5 | Zincate is peeled off | Nitric acid, 25 DEG C, 15 seconds |
6 | Second zincic acid salt treatment | Alkaline zincate treatment fluid, pH12,25 DEG C, 20 seconds |
7 | Electroless phosphorus plating | Acid electroless phosphorus plating solution, pH5.0,85 DEG C, 25 minutes |
8 | Electroless plating gold | Acid electroless plating gold liquid, pH6.5,90 DEG C, 30 minutes |
The fluorescent X-ray film thickness measuring device sold using market, is determined in surface lateral electrode 3a and back side lateral electrode
The non-electrolytic nickel-phosphorus coating 4 and the thickness of electroless plating layer gold 5 formed on 3b.As a result, it is formed on the lateral electrode 3a of surface
Non-electrolytic nickel-phosphorus coating 4 and the thickness of electroless plating layer gold 5 be 7.1 μm and 0.03 μm respectively.In addition, it is formed at the back side
The thickness of non-electrolytic nickel-phosphorus coating 4 and electroless plating layer gold 5 on lateral electrode 3b is 3.9 μm and 0.03 μm respectively.
Next, after making non-electrolytic nickel-phosphorus coating 4 be dissolved into the water containing acid or alkali, determined using ICP in table
The phosphorus concentration of the non-electrolytic nickel-phosphorus coating 4 formed on surface side electrode 3a and back side lateral electrode 3b.As a result, it is formed at face side
The phosphorus concentration of non-electrolytic nickel-phosphorus coating 4 on electrode 3a is 6.9 mass %, the electroless phosphorus being formed on the lateral electrode 3b of the back side
The phosphorus concentration of coating 4 is 8.2 mass %.
Next, the backside down for the semiconductor element 1 for making to produce is placed on platform, by the semiconductor element of tilting
The distance away from platform surface of the end of part 1 determines as the amount of warpage of semiconductor element 1.As a result, amount of warpage is
0.7mm。
Collect the result of embodiment 1 in following tables 2.
[table 2]
(embodiment 2)
In example 2, the semiconductor element 1 with the construction shown in Fig. 1 is made.
First, as surface back side conducting type substrate 2, the thickness for preparing diffusion layer be 70 μm Si substrates (14mm ×
14mm)。
Next, on the surface of Si substrates, the aluminum alloy anode (5 μm of thickness) as surface lateral electrode 3a and guarantor are formed
Cuticula 6, at the back side of Si substrates, form the aluminum alloy anode (1 μm of thickness) as back side lateral electrode 3b.Here, in aluminium alloy
In electrode, shown in table 3 described as follows, at a predetermined ratio containing predetermined element.In addition, make surface lateral electrode 3a surface area
Ratio relative to back side lateral electrode 3b surface area is 0.60.
[table 3]
Next, by method same as Example 1 and under the conditions of carry out each operation, obtain semiconductor element 1.
Similarly to Example 1, the electroless phosphorus formed on surface lateral electrode 3a and back side lateral electrode 3b is determined
The amount of warpage of the thickness and semiconductor element 1 of coating 4 and electroless plating layer gold 5.Its result is shown in following tables 4.
[table 4]
(embodiment 3)
In embodiment 3, the semiconductor element 1 with the construction shown in Fig. 1 is made.
In embodiment 3, the species of the aluminium alloy for surface lateral electrode 3a and back side lateral electrode 3b is changed to carry out
Experiment.Shown in table 5 described as follows, aluminium alloy contains predetermined element at a predetermined ratio.In addition, the table by surface lateral electrode 3a
Area is set to 0.60 relative to the ratio of back side lateral electrode 3b surface area.
[table 5]
Next, by method same as Example 1 and under the conditions of carry out each operation, obtain semiconductor element 1.
Similarly to Example 1, the electroless phosphorus formed on surface lateral electrode 3a and back side lateral electrode 3b is determined
The amount of warpage of the thickness and semiconductor element 1 of coating 4 and electroless plating layer gold 5.Its result is shown in following tables 6.
[table 6]
(embodiment 4)
In example 4, the semiconductor element 1 with the construction shown in Fig. 1 is made.
In example 4, surface lateral electrode 3a surface area is changed relative to the ratio of back side lateral electrode 3b surface area
And bath load is tested.In addition to the ratio and bath load that change the surface area, same as Example 1
Method and under the conditions of, carry out each operation, so as to obtain semiconductor element 1.
Similarly to Example 1, the electroless phosphorus formed on surface lateral electrode 3a and back side lateral electrode 3b is determined
The amount of warpage of the thickness and semiconductor element 1 of coating 4 and electroless plating layer gold 5.Its result is shown in following tables 7.
[table 7]
(embodiment 5)
In embodiment 5, the semiconductor element 1 with the construction shown in Fig. 1 is made.
In embodiment 5, except the ratio by surface lateral electrode 3a surface area relative to back side lateral electrode 3b surface area
Beyond example is set to 0.70 and carries out electroless phosphorus plating with the method shown in Fig. 3, in method same as Example 1 and
Under the conditions of, each operation is carried out, so as to obtain semiconductor element 1.In addition, the dummy material 11 during as electroless phosphorus plating,
Use the material shown in following tables 8.In addition, shown in the distance of back side lateral electrode 3b and dummy material 11 table 8 described as follows.
Similarly to Example 1, the electroless phosphorus formed on surface lateral electrode 3a and back side lateral electrode 3b is determined
The amount of warpage of the thickness and semiconductor element 1 of coating 4 and electroless plating layer gold 5.Its result is shown in following tables 8.
[table 8]
(embodiment 6)
In embodiment 6, the semiconductor element 1 with the construction shown in Fig. 1 is made.
In embodiment 6, except the ratio by surface lateral electrode 3a surface area relative to back side lateral electrode 3b surface area
Beyond example is set to 0.70 and carries out electroless phosphorus plating with the method shown in Fig. 4, in method same as Example 1 and
Under the conditions of, each operation is carried out, so as to obtain semiconductor element 1.In addition, the distance between back side lateral electrode 3b tables 9 described as follows
It is shown.
Similarly to Example 1, the electroless phosphorus formed on surface lateral electrode 3a and back side lateral electrode 3b is determined
The amount of warpage of the thickness and semiconductor element 1 of coating 4 and electroless plating layer gold 5.Its result is shown in following tables 8.
[table 9]
(embodiment 7)
By placing solder and after the semiconductor element 1 obtained in embodiment 1~6 is also placed on thereon in substrate,
With backflow stove heat, the back side lateral electrode 3b of semiconductor element 1 is soldered to substrate.As a result, confirm in solder part not
Emptying aperture be present, and the semiconductor element 1 of soldering is without warpage.
(embodiment 8)
In embodiment 8, surface lateral electrode 3a and the back side lateral electrode 3b non-electrolytic nickel phosphor plating are formed at except changing
Beyond ratio of the thickness and change surface lateral electrode 3a of layer relative to back side lateral electrode 3b surface area, use and embodiment
1 identical method and condition are come after making the semiconductor element 1 with the construction shown in Fig. 1, by same as Example 7
Method, the back side lateral electrode 3b of semiconductor element 1 is soldered to substrate.
Similarly to Example 1, the electroless phosphorus formed on surface lateral electrode 3a and back side lateral electrode 3b is determined
The amount of warpage of the thickness and semiconductor element 1 of coating 4 and electroless plating layer gold 5.In addition, evaluation whether there is sky in solder part
Hole.These results are shown in following tables 10.
[table 10]
As shown in table 10, the thickness of the non-electrolytic nickel-phosphorus coating on surface lateral electrode 3a is formed at relative to be formed at the back of the body
When the ratio of the thickness of non-electrolytic nickel-phosphorus coating on the electrode 3b of surface side is more than 1.0, emptying aperture (sample is not produced in solder part
8-1~8-3), in contrast, when the ratio is less than 1.0, emptying aperture (sample 8-4) is produced in solder part.
In addition, the surface area in surface lateral electrode 3a relative to the ratio of back side lateral electrode 3b surface area is less than 0.85
When, do not produce emptying aperture (sample 8-1~8-3) in solder part, in contrast, when the ratio is more than 0.85, in solder part
Produce emptying aperture (sample 8-4).
It was found from result more than, in accordance with the invention it is possible to which providing can prevent in solder when being installed by soldering
Portion produces the semiconductor element and its manufacture method of emptying aperture.
In addition, this international application is advocated based in Japanese patent application 2015-077528 filed in 6 days April in 2015
Number priority, home quote the full contents of these Japanese patent applications in the application of border.
Claims (8)
- A kind of 1. semiconductor element, formed with non-in the surface lateral electrode and back side lateral electrode of surface back side conducting type substrate It is electrolysed nickel-phosphorus coating and electroless plating layer gold, the semiconductor element is characterised by,The surface lateral electrode and the back side lateral electrode include aluminium or aluminium alloy, andThe thickness for the non-electrolytic nickel-phosphorus coating being formed in the surface lateral electrode is relative to be formed at the back side lateral electrode On the ratio of thickness of the non-electrolytic nickel-phosphorus coating be more than 1.0 and less than 3.5.
- 2. semiconductor element according to claim 1, it is characterised in thatThe aluminium alloy for forming the surface lateral electrode and the back side lateral electrode contains the element more expensive than aluminium.
- 3. semiconductor element according to claim 2, it is characterised in thatThe element ratio contained in the aluminium alloy for forming the surface lateral electrode is forming the back side lateral electrode The element contained in the aluminium alloy is expensive.
- 4. a kind of manufacture method of semiconductor element, surface lateral electrode and back side lateral electrode are being formed at surface back side conducting After type substrate, non-electrolytic is carried out simultaneously to the surface lateral electrode and this two side of the back side lateral electrode using zincate method Nickel phosphor plating is coated with and electroless plating gold, and the manufacture method of the semiconductor element is characterised by,The surface lateral electrode and the back side lateral electrode include aluminium or aluminium alloy, andBy the surface area of the surface lateral electrode relative to the ratio of the surface area of the back side lateral electrode be set to more than 0.3 and Less than 0.85.
- 5. the manufacture method of semiconductor element according to claim 4, it is characterised in thatThe aluminium alloy for forming the surface lateral electrode and the back side lateral electrode contains the element more expensive than aluminium.
- 6. the manufacture method of semiconductor element according to claim 5, it is characterised in thatThe element ratio contained in the aluminium alloy for forming the surface lateral electrode is forming the back side lateral electrode The element contained in the aluminium alloy is expensive.
- 7. the manufacture method of the semiconductor element described in any one in claim 4~6, it is characterised in thatDummy material is being configured with the position of the rear side electrode contraposition to carry out electroless phosphorus plating.
- 8. the manufacture method of the semiconductor element described in any one in claim 4~6, it is characterised in thatPrepare multiple surface back side conducting type substrates formed with the surface lateral electrode and the back side lateral electrode, make The back side lateral electrode of multiple surface back side conducting type substrates carries out electroless phosphorus plating opposite each otherly.
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